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Expression, purification, and characterization of a membrane-associated cyclic oligo-adenylate degrader from Sulfolobus islandicus
Type III CRISPR-cas systems initiate cyclic oligo-adenylate (cOA) signaling to initiate immune response. Previously, we identified that a membrane-associated DHH-DHHA1 family protein from Sulfolobus islandicus efficiently degrades cOA. Here, we provide detailed protocols for expression and purificat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7841402/ https://www.ncbi.nlm.nih.gov/pubmed/33537681 http://dx.doi.org/10.1016/j.xpro.2021.100299 |
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author | Zhao, Ruiliang Yang, Yang Yang, Ke Han, Wenyuan |
author_facet | Zhao, Ruiliang Yang, Yang Yang, Ke Han, Wenyuan |
author_sort | Zhao, Ruiliang |
collection | PubMed |
description | Type III CRISPR-cas systems initiate cyclic oligo-adenylate (cOA) signaling to initiate immune response. Previously, we identified that a membrane-associated DHH-DHHA1 family protein from Sulfolobus islandicus efficiently degrades cOA. Here, we provide detailed protocols for expression and purification of the protein from its native host and a cOA degradation assay with the purified enzyme. The methodology should be of interest for researchers studying Sulfolobus, membrane-associated proteins, or type III CRISPR-cas systems. For complete details on the use and execution of this protocol, please refer to Zhao et al. (2020). |
format | Online Article Text |
id | pubmed-7841402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-78414022021-02-02 Expression, purification, and characterization of a membrane-associated cyclic oligo-adenylate degrader from Sulfolobus islandicus Zhao, Ruiliang Yang, Yang Yang, Ke Han, Wenyuan STAR Protoc Protocol Type III CRISPR-cas systems initiate cyclic oligo-adenylate (cOA) signaling to initiate immune response. Previously, we identified that a membrane-associated DHH-DHHA1 family protein from Sulfolobus islandicus efficiently degrades cOA. Here, we provide detailed protocols for expression and purification of the protein from its native host and a cOA degradation assay with the purified enzyme. The methodology should be of interest for researchers studying Sulfolobus, membrane-associated proteins, or type III CRISPR-cas systems. For complete details on the use and execution of this protocol, please refer to Zhao et al. (2020). Elsevier 2021-01-25 /pmc/articles/PMC7841402/ /pubmed/33537681 http://dx.doi.org/10.1016/j.xpro.2021.100299 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Protocol Zhao, Ruiliang Yang, Yang Yang, Ke Han, Wenyuan Expression, purification, and characterization of a membrane-associated cyclic oligo-adenylate degrader from Sulfolobus islandicus |
title | Expression, purification, and characterization of a membrane-associated cyclic oligo-adenylate degrader from Sulfolobus islandicus |
title_full | Expression, purification, and characterization of a membrane-associated cyclic oligo-adenylate degrader from Sulfolobus islandicus |
title_fullStr | Expression, purification, and characterization of a membrane-associated cyclic oligo-adenylate degrader from Sulfolobus islandicus |
title_full_unstemmed | Expression, purification, and characterization of a membrane-associated cyclic oligo-adenylate degrader from Sulfolobus islandicus |
title_short | Expression, purification, and characterization of a membrane-associated cyclic oligo-adenylate degrader from Sulfolobus islandicus |
title_sort | expression, purification, and characterization of a membrane-associated cyclic oligo-adenylate degrader from sulfolobus islandicus |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7841402/ https://www.ncbi.nlm.nih.gov/pubmed/33537681 http://dx.doi.org/10.1016/j.xpro.2021.100299 |
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